Exosome detecting device for detection and by-stage judgment of non-small-cell lung cancer and application

A non-small cell lung cancer and detection device technology, applied in the field of medical detection, can solve problems such as difficulty

Pending Publication Date: 2019-12-03
THE NAT CENT FOR NANOSCI & TECH NCNST OF CHINA
View PDF2 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the small size of nanometers makes the separation, purification and detection of exosomes face great challenges. In ad

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Exosome detecting device for detection and by-stage judgment of non-small-cell lung cancer and application
  • Exosome detecting device for detection and by-stage judgment of non-small-cell lung cancer and application
  • Exosome detecting device for detection and by-stage judgment of non-small-cell lung cancer and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0107] This example is used to illustrate the extraction of exosomes from the cell culture supernatant.

[0108] 1. Cell material used

[0109] Colorectal cancer cell line SW620, three lung cancer cell lines A549, H1975, H1650.

[0110] 2. The specific steps include:

[0111] 1) When the cells grow to a density of 60%, replace with the culture medium prepared from the serum that has previously deducted exosomes, and place it in the cell culture incubator for 48 hours.

[0112] Wherein, the preparation of the culture medium by deducting the serum of exosomes comprises the following steps:

[0113] ① Add the serum to the basal medium, so that the concentration of FBS in the cell culture medium is 20%;

[0114] ②Ultracentrifuge the cell culture medium overnight at 4°C with a centrifugal force of 100,000 g;

[0115] ③ After the ultracentrifugation, collect the supernatant, dilute the medium containing 20% ​​FBS with the basal medium to a FBS concentration of 10%, and add 1% do...

Embodiment 2

[0123] This example is used to illustrate the morphology and size characterization of the extracted exosomes.

[0124] 1. Transmission Electron Microscopy (TEM) Characterization

[0125] Take 10 μL of exosomes extracted according to the method in Example 1 and drop them on the ultra-thin carbon support membrane (Beijing Zhongjingkeyi Technology Co., Ltd., China), dry naturally at room temperature for 30 min, absorb the floating liquid, and add 10 μL of PBS dropwise Put the buffer solution on the support membrane, suck it off after 1min, add 10uL of 1% glutaraldehyde in the fixative solution dropwise, let it stand for 5min, absorb the floating solution, add the rich dye 2% uranyl acetate on the support membrane dropwise, and stain After 1 min, the filter paper was sucked to remove the floating liquid, and after drying at room temperature for 24 h, it was observed with a Hitachi High-Tech 7700 transmission electron microscope produced by Hitachi, Japan at an accelerating voltage...

Embodiment 3

[0134] This example is used to illustrate the preparation and morphology characterization of exosome-microsphere complexes.

[0135] 1. Quantification of exosome protein

[0136] Take 20 μL of exosomes extracted according to the method of Example 1 in a centrifuge tube, add 20 μL of protein lysate (containing protease inhibitors), mix well, and lyse on ice for 1 hour, using the BCA protein quantification kit produced by Solebol Company The protein content of exosomes was quantified.

[0137] 2. Preparation of exosome-microsphere complexes

[0138] 1) According to the results of protein quantification, take exosomes with a protein content of 10 μg, mix them well with 2.5uL microspheres, incubate at room temperature for 15min, add PBS buffer to a total volume of 250ul, and incubate overnight at 4°C.

[0139] 2) Add 28 μL of glycine with a concentration of 1M to the above mixture, so that the final concentration of glycine is 100 mM, and react at room temperature for 30 minutes...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
Size distributionaaaaaaaaaa
Sizeaaaaaaaaaa
Login to view more

Abstract

The invention provides an exosome detecting device for detection and by-stage judgment of non-small-cell lung cancer and application of the exosome detecting device. The exosome detecting device comprises an exosome extracting mechanism, an exosome representation mechanism, an exosome protein expression capacity information determining mechanism and an exosome expression capacity information analysis mechanism. The exosome detecting device disclosed by the invention is easy and simple to handle and low in cost, can realize real-time tracking of the illness state, and can adjust a treatment scheme in time according to the development of disease, and the exosome detecting device has good application prospects in the respect of disease early screening and individualized medical care.

Description

technical field [0001] The invention belongs to the field of medical detection, and in particular relates to an exosome detection device and application for non-small cell lung cancer detection and staging judgment. Background technique [0002] Lung cancer is the malignant tumor with the fastest growing morbidity and mortality in the world, the greatest threat to the health and life of the population, and the number one cause of cancer death in the world. Among various types of lung cancer, non-small cell lung cancer (NSCLC) accounts for about 85%, and is the most common lung cancer. It mainly includes adenocarcinoma, squamous cell carcinoma (squamous cell carcinoma of the lung), and large cell undifferentiated carcinoma. Lung adenocarcinoma is the most important type, accounting for about 40%. [0003] Clinically, pathological diagnosis is still the "gold standard" for diagnosing lung cancer. Pathological diagnosis is used to determine the type of lung cancer, assisting o...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C12Q1/6886C12Q1/6851
CPCC12Q1/6886C12Q1/6851C12Q2600/156C12Q2600/112
Inventor 杨延莲李文哲朱凌王华艺王琛
Owner THE NAT CENT FOR NANOSCI & TECH NCNST OF CHINA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap